A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662290



Internal ID9581709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119358268..119358414hg38UCSC Ensembl
chr11:119228978..119229124hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6540698, essv6178192
SamplesHG00448, HG00479
Known GenesUSP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662290
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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